MGP Database

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MGP004151

Ontology/Pathway Information

Entrez Gene ID10166
Gene Namesolute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15
Gene Symbol SLC25A15
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0016021 TAS:ProtIncCintegral component of membrane
GO:0005743 TAS:ReactomeCmitochondrial inner membrane
GO:0000064 TAS:ProtIncFL-ornithine transmembrane transporter activity
GO:0006520 TAS:ProtIncPcellular amino acid metabolic process
GO:0034641 TAS:ReactomePcellular nitrogen compound metabolic process
GO:1903352 TAS:GOCPL-ornithine transmembrane transport
GO:0000066 TAS:ProtIncPmitochondrial ornithine transport
GO:0044281 TAS:ReactomePsmall molecule metabolic process
GO:0000050 TAS:ReactomePurea cycle
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_111217Metabolism
REACT_13Metabolism of amino acids and derivatives
REACT_847Urea cycle
SMP Pathway Links
SMP IDDescription
SMP00020Arginine and Proline Metabolism
SMP00362Arginine: Glycine Amidinotransferase Deficiency (AGAT Deficiency)
SMP00357Argininemia
SMP00003Argininosuccinic Aciduria
SMP00002Carbamoyl Phosphate Synthetase Deficiency
SMP00001Citrullinemia Type I
SMP00504Creatine deficiency, guanidinoacetate methyltransferase deficiency
SMP00188Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency)
SMP00506Hyperornithinemia-hyperammonemia-homocitrullinuria [HHH-syndrome]
SMP00505Hyperornithinemia with gyrate atrophy (HOGA)
SMP00361Hyperprolinemia Type I
SMP00360Hyperprolinemia Type II
SMP00507L-arginine:glycine amidinotransferase deficiency
SMP00363Ornithine Aminotransferase Deficiency (OAT Deficiency)
SMP00205Ornithine Transcarbamylase Deficiency (OTC Deficiency)
SMP00207Prolidase Deficiency (PD)
SMP00208Prolinemia Type II
SMP00059Urea Cycle
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